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rs367543016

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs367543016(G;G)
Make rs367543016(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90769233
GeneBLM
is asnp
is mentioned by
dbSNPrs367543016
ebirs367543016
HLIrs367543016
Exacrs367543016
Varsomers367543016
Maprs367543016
PheGenIrs367543016
hapmaprs367543016
1000 genomesrs367543016
hgdprs367543016
ensemblrs367543016
gopubmedrs367543016
geneviewrs367543016
scholarrs367543016
googlers367543016
pharmgkbrs367543016
gwascentralrs367543016
openSNPrs367543016
23andMers367543016
23andMe allrs367543016
SNP Nexus

SNPshotrs367543016
SNPdbers367543016
MSV3drs367543016
GWAS Ctlgrs367543016
Max Magnitude0
ClinVar
Risk rs367543016(G;G)
Alt rs367543016(G;G)
Reference rs367543016(T;T)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91312463T>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034896.1,